Imidazo[1,2-b][1,2,4]triazines as c-met inhibitors

ABSTRACT

The present invention relates to imidazo[1,2-b][1,2,4]triazines that are inhibitors of c-Met and are useful in the treatment of c-Met associated diseases including cancer.

RELATED APPLICATION

This application is a Continuation of U.S. Application Serial No.15/969,519 filed May 2, 2018, which application is a Continuation ofU.S. application Ser. No. 14/918,879 filed Oct. 21, 2015, now issued asU.S. Pat. No. 9,988,387, which application is a Continuation of U.S.application Ser. No. 13/915,702, filed Jun. 12, 2013, now issued as U.S.Pat. No. 9,221,824, which application is a Continuation of U.S.application Ser. No. 13/019,718 filed Feb. 2, 2011 which applicationclaims priority to U.S. Provisional Application No. 61/300,946, filedFeb. 3, 2010, titled “IMIDAZO[1,2-b][1,2,4]TRIAZINES AS C-METINHIBITORS.” The contents of any patents, patent applications, andreferences cited throughout this specification are hereby incorporatedby reference in their entireties.

FIELD OF THE INVENTION

The present invention relates to imidazo[1,2-b][1,2,4]triazines that areinhibitors of c-Met and are useful in the treatment of c-Met associateddiseases including cancer.

BACKGROUND OF THE INVENTION

Protein kinases (PKs) are a group of enzymes that regulate diverse,important biological processes including cell growth, survival anddifferentiation, organ formation and morphogenesis, neovascularization,tissue repair and regeneration, among others. Protein kinases exerttheir physiological functions through catalyzing the phosphorylation ofproteins (or substrates) and thereby modulating the cellular activitiesof the substrates in various biological contexts. In addition to thefunctions in normal tissues/organs, many protein kinases also play morespecialized roles in a host of human diseases including cancer. A subsetof protein kinases (also referred to as oncogenic protein kinases), whendysregulated, can cause tumor formation and growth, and furthercontribute to tumor maintenance and progression (Blume-Jensen P et al,Nature 2001, 411(6835):355-365). Thus far, oncogenic protein kinasesrepresent one of the largest and most attractive groups of proteintargets for cancer intervention and drug development.

c-Met, a proto-oncogene, is a member of a distinct subfamily ofheterodimeric receptor tyrosine kinases which include Met, Ron, and Sea(Birchmeier, C. et al., Nat. Rev. Mol. Cell Biol. 2003, 4(12):915-925;Christensen, J. G. et al., Cancer Lett. 2005, 225(1):1-26). The onlyhigh affinity ligand for c-Met is the hepatocyte growth factor (HGF),also known as scatter factor (SF). Binding of HGF to c-Met inducesactivation of the receptor via autophosphorylation resulting in anincrease of receptor dependent signaling. Both c-Met and HGF are widelyexpressed in a variety of organs, but their expression is normallyconfined to the cells of epithelial and mesenchymal origin,respectively. The biological functions of c-Met (or c-Met signalingpathway) in normal tissues and human malignancies such as cancer havebeen well documented (Christensen, J. G. et al., Cancer Lett. 2005,225(1):1-26; Corso, S. et al., Trends in Mol. Med. 2005, 11(6):284-292).

HGF and c-Met are each required for normal mammalian development, andabnormalities reported in both HGF- and c-Met-null mice are consistentwith proximity of embryonic expression and epithelial-mesenchymaltransition defects during organ morphogenesis (Christensen, J. G. etal., Cancer Lett. 2005, 225(1):1-26). Consistent with these findings,the transduction of signaling and subsequent biological effects ofHGF/c-Met pathway have been shown to be important forepithelial-mesenchymal interaction and regulation of cell migration,invasion, cell proliferation and survival, angiogenesis, morphogenesisand organization of three-dimensional tubular structures (e.g. renaltubular cells, gland formation) during development. The specificconsequences of c-Met pathway activation in a given cell/tissue arehighly context-dependent.

Dysregulated c-Met pathway plays important and sometimes causative (inthe case of genetic alterations) roles in tumor formation, growth,maintenance and progression (Birchmeier, C. et al., Nat. Rev. Mol. Cell.Biol. 2003, 4(12):915-925; Boccaccio, C. et al., Nat. Rev. Cancer 2006,6(8):637-645; Christensen, J. G. et al., Cancer Lett. 2005,225(1):1-26). HGF and/or c-Met are overexpressed in significant portionsof most human cancers, and are often associated with poor clinicaloutcomes such as more aggressive disease, disease progression, tumormetastasis and shortened patient survival. Further, patients with highlevels of HGF/c-Met proteins are more resistant to chemotherapy andradiotherapy. In addition to the abnormal HGF/c-Met expression, thec-Met receptor can also be activated in cancer patients through geneticmutations (both germline and somatic) and gene amplification. Althoughgene amplification and mutations are the most common genetic alterationsthat have been reported in patients, the receptor can also be activatedby deletions, truncations, gene rearrangement, as well as abnormalreceptor processing and defective negative regulatory mechanisms.

The various cancers in which c-Met is implicated include, but are notlimited to: carcinomas (e.g., bladder, breast, cervical,cholangiocarcinoma, colorectal, esophageal, gastric, head and neck,kidney, liver, lung, nasopharygeal, ovarian, pancreas, prostate,thyroid); musculoskeletal sarcomas (e.g., osteosarcaoma, synovialsarcoma, rhabdomyosarcoma); soft tissue sarcomas (e.g.,MFH/fibrosarcoma, leiomyosarcoma, Kaposi's sarcoma); hematopoieticmalignancies (e.g., multiple myeloma, lymphomas, adult T cell leukemia,acute myelogenous leukemia, chronic myeloid leukemia); and otherneoplasms (e.g., glioblastomas, astrocytomas, melanoma, mesothelioma andWilm's tumor (www.vai.org/met/; Christensen, J. G. et al., Cancer Lett.2005, 225(1):1-26).

The notion that the activated c-Met pathway contributes to tumorformation and progression and could be a good target for effectivecancer intervention has been further solidified by numerous preclinicalstudies (Birchmeier, C. et al., Nat. Rev. Mol. Cell Biol. 2003,4(12):915-925; Christensen, J. G. et al., Cancer Lett. 2005,225(1):1-26; Corso, S. et al., Trends in Mol. Med. 2005, 11(6):284-292).For example, studies showed that the tpr-met fusion gene, overexpressionof c-met and activated c-met mutations all caused oncogenictransformation of various model cell lines and resulted in tumorformation and metastasis in mice. More importantly, significantanti-tumor (sometimes tumor regression) and anti-metastasis activitieshave been demonstrated in vitro and in vivo with agents thatspecifically impair and/or block HGF/c-Met signaling. Those agentsinclude anti-HGF and anti-c-Met antibodies, HGF peptide antagonists,decoy c-Met receptor, c-Met peptide antagonists, dominant negative c-Metmutations, c-Met specific antisense oligonucleotides and ribozymes, andselective small molecule c-Met kinase inhibitors (Christensen, J. G. etal., Cancer Lett. 2005, 225(1):1-26).

In addition to the established role in cancer, abnormal HGF/c-Metsignaling is also implicated in atherosclerosis, lung fibrosis, renalfibrosis and regeneration, liver diseases, allergic disorders,inflammatory and autoimmune disorders, cerebrovascular diseases,cardiovascular diseases, conditions associated with organtransplantation (Ma, H. et al., Atherosclerosis. 2002, 164(1):79-87;Crestani, B. et al., Lab. Invest. 2002, 82(8):1015-1022; Sequra-Flores,A. A. et al., Rev. Gastroenterol. Mex. 2004, 69(4)243-250; Morishita, R.et al., Curr. Gene Ther. 2004, 4(2)199-206; Morishita, R. et al.,Endocr. J. 2002, 49(3)273-284; Liu, Y., Curr. Opin. Nephrol. Hypertens.2002, 11(1):23-30; Matsumoto, K. et al., Kidney Int. 2001,59(6):2023-2038; Balkovetz, D. F. et al., Int. Rev. Cytol. 1999,186:225-250; Miyazawa, T. et al., J. Cereb. Blood Flow Metab. 1998,18(4)345-348; Koch, A.E. et al., Arthritis Rheum. 1996, 39(9):1566-1575;Futamatsu, H. et al., Circ. Res. 2005, 96(8)823-830; Eguchi, S. et al.,Clin. Transplant. 1999, 13(6)536-544).

New or improved forms of existing agents which inhibit kinases such asc-Met are continually needed for developing more effectivepharmaceuticals to treat cancer and other diseases. The compounds andsalts described herein are directed toward these needs and other ends.

SUMMARY OF THE INVENTION

The present invention provides, inter alia, the following compoundswhich are c-Met inhibitors:

2-fluoro-N-[(2R)-2-hydroxypropyl]-4-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]benzamide(Formula I);

2-chloro-N-methyl-4-(7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl)benzamide(Formula II);

2-chloro-N-[(1S)-1-(5-methyl-1,2,4-oxadiazol-3-yl)ethyl]-4-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]benzamide(Formula III);

N-methyl-5-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]pyridine-2-carboxamide(Formula IV); and

N,2-dimethyl-4-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]benzamide(Formula V).

The present invention further provides a pharmaceutically acceptablesalt of any one of the aforementioned compounds.

The present invention further provides a method of inhibiting activityof c-Met kinase comprising contacting the kinase with a compound or saltof the invention.

The present invention further provides a method of inhibiting theHGF/c-Met kinase signaling pathway in a cell comprising contacting thecell with a compound or salt of the invention.

The present invention further provides a method of inhibiting theproliferative activity of a cell comprising contacting the cell with acompound or salt of the invention.

The present invention further provides a method of inhibiting tumorgrowth in a patient comprising administering to the patient atherapeutically effective amount of a compound or salt of the invention.

The present invention further provides a method of inhibiting tumormetastasis in a patient comprising administering to the patient atherapeutically effective amount of a compound or salt of the invention.

The present invention further provides a method of treating a disease ina patient, wherein the disease is associated with dysregulation of theHGF/c-MET signaling pathway, comprising administering to the patient atherapeutically effective amount of a compound or salt of the invention.

The present invention further provides a method of treating cancer in apatient comprising administering to the patient a therapeuticallyeffective amount of a compound or salt of the invention.

The present invention provides a compound of the invention for use intherapy.

The present invention provides the use of a compound of the inventionfor the preparation of a medicament for use in therapy. In oneembodiment, the present invention provides the use of any one ofcompounds of Formula I, II, III, IV, or V for the preparation of amedicament for use in treatment of cancer.

DETAILED DESCRIPTION

The present invention provides, inter alia, the following compoundswhich are c-Met inhibitors:

2-fluoro-N-[(2R)-2-hydroxypropyl]-4-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]benzamide(Formula I);

2-chloro-N-methyl-4-(7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl)benzamide(Formula II);

2-chloro-N-[(1S)-1-(5-methyl-1,2,4-oxadiazol-3-yl)ethyl]-4-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]benzamide(Formula III);

N-methyl-5-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]pyridine-2-carboxamide(Formula IV); and

N,2-dimethyl-4-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]benzamide(Formula V).

Here and elsewhere, where discrepancies exist between a compound's nameand a compound's structure, the chemical structure will control.

The present invention further provides pharmaceutically acceptable saltsof any of the aforementioned compounds.

The compounds described herein can be asymmetric (e.g., having one ormore stereocenters). All stereoisomers, such as enantiomers anddiastereomers, are intended unless otherwise indicated. Compounds of thepresent invention that contain asymmetrically substituted carbon atomscan be isolated in optically active or racemic forms.

Compounds of the invention also include tautomeric forms. Tautomericforms result from the swapping of a single bond with an adjacent doublebond together with the concomitant migration of a proton. Tautomericforms include prototropic tautomers which are isomeric protonationstates having the same empirical formula and total charge. Exampleprototropic tautomers include ketone—enol pairs, amide—imidic acidpairs, lactam—lactim pairs, amide—imidic acid pairs, enamine—iminepairs, and annular forms where a proton can occupy two or more positionsof a heterocyclic system, for example, 1H- and 3H-imidazole, 1H-, 2H-and 4H-1,2,4-triazole, 1H- and 2H-isoindole, and 1H- and 2H-pyrazole.Tautomeric forms can be in equilibrium or sterically locked into oneform by appropriate substitution.

Compounds of the invention also include all isotopes of atoms occurringin the intermediates or final compounds. Isotopes include those atomshaving the same atomic number but different mass numbers. For example,isotopes of hydrogen include tritium and deuterium.

In some embodiments, the compounds of the invention, or their salts, aresubstantially isolated. By “substantially isolated” is meant that thecompound or salt is at least partially or substantially separated fromthe environment in which it was formed or detected. Partial separationcan include, for example, a composition enriched in the compound of theinvention. Substantial separation can include compositions containing atleast about 50%, at least about 60%, at least about 70%, at least about80%, at least about 90%, at least about 95%, at least about 97%, or atleast about 99% by weight of the compound of the invention, or saltthereof.

The present invention also includes pharmaceutically acceptable salts ofthe compounds described herein. As used herein, “pharmaceuticallyacceptable salts” refers to derivatives of the disclosed compoundswherein the parent compound is modified by converting an existing acidor base moiety to its salt form. Examples of pharmaceutically acceptablesalts include, but are not limited to, mineral or organic acid salts ofbasic residues such as amines; alkali or organic salts of acidicresidues such as carboxylic acids; and the like. The pharmaceuticallyacceptable salts of the present invention include the conventionalnon-toxic salts of the parent compound formed, for example, fromnon-toxic inorganic or organic acids. The pharmaceutically acceptablesalts of the present invention can be synthesized from the parentcompound which contains a basic or acidic moiety by conventionalchemical methods. Generally, such salts can be prepared by reacting thefree acid or base forms of these compounds with a stoichiometric amountof the appropriate base or acid in water or in an organic solvent, or ina mixture of the two; generally, nonaqueous media like ether, ethylacetate, ethanol, isopropanol, or acetonitrile are preferred. Lists ofsuitable salts are found in Remington's Pharmaceutical Sciences, 17^(th)ed., Mack Publishing Company, Easton, Pa., 1985, p. 1418 and Journal ofPharmaceutical Science, 66, 2 (1977), each of which is incorporatedherein by reference in its entirety.

The phrase “pharmaceutically acceptable” is employed herein to refer tothose compounds, materials, compositions, and/or dosage forms which are,within the scope of sound medical judgment, suitable for use in contactwith the tissues of human beings and animals without excessive toxicity,irritation, allergic response, or other problem or complication,commensurate with a reasonable benefit/risk ratio.

Methods of Use

The compounds of the present invention can act as inhibitors of c-Met.Treatment of a cell (in vitro or in vivo) that expresses c-Met with acompound of the invention can result in inhibiting the ligand/kinasesignaling pathway and inhibiting downstream events related to thesignaling pathway such as cellular proliferation and increased cellmotility. For example, the compounds of the invention can block and/orimpair the biochemical and biological processes resulting from c-Metpathway activation, including, but not limited to, c-Met kinaseactivation (e.g. c-Met phosphorylation) and signaling (activation andrecruitment of cellular substrates such as Gab1, Grb2, Shc and c-Cbl andsubsequent activation of a number of signal transducers including PI-3kinase, PLC-γ, STATs, ERK1/2 and FAK), cell proliferation and survival,cell motility, migration and invasion, metastasis, angiogenesis, and thelike. Thus, the present invention further provides methods of inhibitinga ligand/kinase signaling pathway such as the HGF/c-Met kinase signalingpathway in a cell by contacting the cell with a compound of theinvention. The present invention further provides methods of inhibitingproliferative activity of a cell or inhibiting cell motility bycontacting the cell with a compound of the invention.

The present invention further provides methods of treating diseasesassociated with a dysregulated c-Met kinase signaling pathway, includingabnormal activity and/or overexpression of the c-Met, in an individual(e.g., patient) by administering to the individual in need of suchtreatment a therapeutically effective amount or dose of a compound ofthe present invention or a pharmaceutical composition thereof. In someembodiments, the dysregulated kinase is overexpressed in the diseasedtissue of the patient. In some embodiments, the dysregulated kinase isabnormally active in the diseased tissue of the patient. Dysregulationof c-Met and the HGF/c-Met signaling pathway is meant to includeactivation of the enzyme through various mechanisms including, but notlimited to, HGF-dependent autocrine and paracrine activation, c-met geneoverexpression and amplification, point mutations, deletions,truncations, rearrangement, as well as abnormal c-Met receptorprocessing and defective negative regulatory mechanisms.

In some embodiments, the compounds of the invention are useful intreating diseases such as cancer, atherosclerosis, lung fibrosis, renalfibrosis and regeneration, liver disease, allergic disorder,inflammatory disease, autoimmune disorder, cerebrovascular disease,cardiovascular disease, or condition associated with organtransplantation. In further embodiments, the compounds of the inventioncan be useful in methods of inhibiting tumor growth or metastasis of atumor in a patient.

Example cancers treatable by the methods herein include bladder cancer,breast cancer, cervical cancer, cholangiocarcinoma cancer, colorectalcancer, esophageal cancer, gastric cancer, head and neck cancer, cancerof the kidney, liver cancer, lung cancer, nasopharygeal cancer, ovariancancer, pancreatic cancer, prostate cancer, thyroid cancer,osteosarcoma, synovial sarcoma, rhabdomyosarcoma, MFH/fibrosarcoma,leiomyosarcoma, Kaposi's sarcoma, multiple myeloma, lymphoma, adult Tcell leukemia, acute myelogenous leukemia, chronic myeloid leukemia.glioblastoma, astrocytoma, melanoma, mesothelioma, or Wilm's tumor, andthe like.

Thus, in one embodiment, provided herein is a method of treating cancerin a subject, comprising administering to the subject2-fluoro-N-[(2R)-2-hydroxypropyl]-4-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]benzamide,or a pharmaceutically acceptable salt thereof, such that the cancer istreated.

In another embodiment, provided herein is a method of treating cancer ina subject, comprising administering to the subject2-chloro-N-methyl-4-(7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl)benzamide,or a pharmaceutically acceptable salt thereof, such that the cancer istreated.

In another embodiment, provided herein is a method of treating cancer ina subject, comprising administering to the subject2-chloro-N-[(1S)-1-(5-methyl-1,2,4-oxadiazol-3-yl)ethyl]-4-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]benzamide,or a pharmaceutically acceptable salt thereof, such that the cancer istreated.

In another embodiment, provided herein is a method of treating cancer ina subject comprising administering to the subjectN-methyl-5-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]pyridine-2-carboxamide,or a pharmaceutically acceptable salt thereof, such that the cancer istreated.

In another embodiment, provided herein is a method of treating cancer ina subject in need thereof, comprising administering to the subjectN,2-dimethyl-4-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]benzamide,or a pharmaceutically acceptable salt thereof, such that the cancer istreated.

Thus, in one embodiment, provided herein is a method of inhibiting tumorgrowth in a subject in need thereof, comprising administering to thesubject2-fluoro-N-[(2R)-2-hydroxypropyl]-4-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]benzamide,or a pharmaceutically acceptable salt thereof.

In another embodiment, provided herein is a method of inhibiting tumorgrowth in a subject in need thereof, comprising administering to thesubject2-chloro-N-methyl-4-(7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl)benzamide,or a pharmaceutically acceptable salt thereof.

In another embodiment, provided herein is a method of inhibiting tumorgrowth in a subject in need thereof, comprising administering to thesubject2-chloro-N-[(1S)-1-(5-methyl-1,2,4-oxadiazol-3-ypethyl]-4-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]benzamide,or a pharmaceutically acceptable salt thereof.

In another embodiment, provided herein is a method of inhibiting tumorgrowth in a subject in need thereof, comprising administering to thesubjectN-methyl-5-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]pyridine-2-carboxamide,or a pharmaceutically acceptable salt thereof, such that the cancer istreated.

In another embodiment, provided herein is a method of inhibiting tumorgrowth in a subject in need thereof, comprising administering to thesubjectN,2-dimethyl-4-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]benzamide,or a pharmaceutically acceptable salt thereof.

As used herein, the term “cell” is meant to refer to a cell that is invitro, ex vivo or in vivo. In some embodiments, an ex vivo cell can bepart of a tissue sample excised from an organism such as a mammal. Insome embodiments, an in vitro cell can be a cell in a cell culture. Insome embodiments, an in vivo cell is a cell living in an organism suchas a mammal.

As used herein, the term “contacting” refers to the bringing together ofindicated moieties in an in vitro system or an in vivo system. Forexample, “contacting” a compound of the invention with a protein kinaseincludes the administration of a compound of the present invention to anindividual or patient, such as a human, as well as, for example,introducing a compound of the invention into a sample containing acellular or purified preparation of the protein kinase.

As used herein, the term “individual” or “patient,” usedinterchangeably, refers to any animal, including mammals, preferablymice, rats, other rodents, rabbits, dogs, cats, swine, cattle, sheep,horses, or primates, and most preferably humans.

As used herein, the phrase “therapeutically effective amount” refers tothe amount of active compound or pharmaceutical agent that elicits thebiological or medicinal response that is being sought in a tissue,system, animal, individual or human by a researcher, veterinarian,medical doctor or other clinician, which includes one or more of thefollowing: (1) preventing the disease; for example, preventing adisease, condition or disorder in an individual who may be predisposedto the disease, condition or disorder but does not yet experience ordisplay the pathology or symptomatology of the disease; (2) inhibitingthe disease; for example, inhibiting a disease, condition or disorder inan individual who is experiencing or displaying the pathology orsymptomatology of the disease, condition or disorder; and (3)ameliorating the disease; for example, ameliorating a disease, conditionor disorder in an individual who is experiencing or displaying thepathology or symptomatology of the disease, condition or disorder (i.e.,reversing the pathology and/or symptomatology) such as decreasing theseverity of disease.

The term “treated,” “treating” or “treatment” includes the diminishmentor alleviation of at least one symptom associated with the activity ofc-Met kinase, the HGF/c-Met kinase signaling pathway, and/or theproliferative activity of a cell. The term “treated,” “treating” or“treatment” as used in reference to a disease or condition shall mean tointervene in such disease or condition so as to prevent or slow thedevelopment of, prevent or slow the progression of, halt the progressionof, or eliminate the disease or condition.

The term “use” includes any one or more of the following embodiments ofthe invention, respectively: the use in the treatment of a disorder; theuse for the manufacture of pharmaceutical compositions for use in thetreatment of a disorder, e.g., in the manufacture of a medicament;methods of use of compounds of the invention in the treatment of thesediseases; pharmaceutical preparations having compounds of the inventionfor the treatment of these diseases; and compounds of the invention foruse in the treatment of these diseases; as appropriate and expedient, ifnot stated otherwise. In particular, diseases to be treated and are thuspreferred for use of a compound of the present invention are selectedfrom diseases associated with the activity of c-Met kinase, theHGF/c-Met kinase signaling pathway, and/or the proliferative activity ofa cell, and cancer.

Combination Therapy

One or more additional pharmaceutical agents or treatment methods suchas, for example, chemotherapeutics, anti-cancer agents, cytotoxicagents, or anti-cancer therapies (e.g., radiation, hormone, etc.), canbe used in combination with the compounds and salts of the presentinvention for treatment of the diseases, disorders or conditionsdescribed herein. The agents or therapies can be administered togetherwith the compounds or salts of the invention (e.g., combined into asingle dosage form), or the agents or therapies can be administeredsimultaneously or sequentially by separate routes of administration.

Suitable anti-cancer agents include kinase inhibiting agents includingtrastuzumab (Herceptin), imatinib (Gleevec), gefitinib (Iressa),erlotinib hydrochloride (Tarceva), cetuximab (Erbitux), bevacizumab(Avastin), sorafenib (Nexavar), sunitinib (Sutent), and RTK inhibitorsdescribed in, for example, WO 2005/004808, WO 2005/004607, WO2005/005378, WO 2004/076412, WO 2005/121125, WO 2005/039586, WO2005/028475, WO 2005/040345, WO 2005/039586, WO 2003/097641, WO2003/087026, WO 2005/040154, WO 2005/030140, WO 2006/014325, WO 2005/070891, WO 2005/073224, WO 2005/113494, and US Pat. App. Pub. Nos.2005/0085473, 2006/0046991, and 2005/0075340.

Suitable chemotherapeutic or other anti-cancer agents further include,for example, alkylating agents (including, without limitation, nitrogenmustards, ethylenimine derivatives, alkyl sulfonates, nitrosoureas andtriazenes) such as uracil mustard, chlormethine, cyclophosphamide(Cytoxan™), ifosfamide, melphalan, chlorambucil, pipobroman,triethylene-melamine, triethylenethiophosphoramine, busulfan,carmustine, lomustine, streptozocin, dacarbazine, and temozolomide.

Suitable chemotherapeutic or other anti-cancer agents further include,for example, antimetabolites (including, without limitation, folic acidantagonists, pyrimidine analogs, purine analogs and adenosine deaminaseinhibitors) such as methotrexate, 5-fluorouracil, floxuridine,cytarabine, 6-mercaptopurine, 6-thioguanine, fludarabine phosphate,pentostatine, and gemcitabine.

Suitable chemotherapeutic or other anti-cancer agents further include,for example, certain natural products and their derivatives (forexample, vinca alkaloids, antitumor antibiotics, enzymes, lymphokinesand epipodophyllotoxins) such as vinblastine, vincristine, vindesine,bleomycin, dactinomycin, daunorubicin, doxorubicin, epirubicin,idarubicin, ara-C, paclitaxel (Taxol™), mithramycin, deoxyco-formycin,mitomycin-C, L-asparaginase, interferons (especially IFN-a), etoposide,and teniposide.

Other cytotoxic agents include navelbene, CPT-11, anastrazole,letrazole, capecitabine, reloxafine, cyclophosphamide, ifosamide, anddroloxafine.

Also suitable are cytotoxic agents such as epidophyllotoxin; anantineoplastic enzyme; a topoisomerase inhibitor; procarbazine;mitoxantrone; platinum coordination complexes such as cis-platin andcarboplatin; biological response modifiers; growth inhibitors;antihormonal therapeutic agents; leucovorin; tegafur; and haematopoieticgrowth factors.

Other anti-cancer agent(s) include antibody therapeutics such astrastuzumab (Herceptin), antibodies to costimulatory molecules such asCTLA-4, 4-1BB and PD-1, or antibodies to cytokines (IL-10, TGF-β, etc.).Further antibody therapeutics include antibodies to tyrosine kinasesand/or their ligands such as anti-HGF antibodies and/or anti-c-Metantibodies. The term “antibody” is meant to include whole antibodies(e.g., monoclonal, polyclonal, chimeric, humanized, human, etc.) as wellas antigen-binding fragments thereof.

Other anti-cancer agents also include those that block immune cellmigration such as antagonists to chemokine receptors, including CCR2 andCCR4.

Other anti-cancer agents also include those that augment the immunesystem such as adjuvants or adoptive T cell transfer.

Other anti-cancer agents include anti-cancer vaccines such as dendriticcells, synthetic peptides, DNA vaccines and recombinant viruses.

Methods for the safe and effective administration of most of the aboveagents are known to those skilled in the art. In addition, theiradministration is described in the standard literature. For example, theadministration of many of the chemotherapeutic agents is described inthe “Physicians' Desk Reference” (PDR, e.g., 1996 edition, MedicalEconomics Company, Montvale, N.J.), the disclosure of which isincorporated herein by reference as if set forth in its entirety.

Pharmaceutical Formulations and Dosage Forms

When employed as pharmaceuticals, the compounds or salts of theinvention can be administered in the form of pharmaceutical compositionscorresponding to a combination of a compound of the invention (or saltthereof) and a pharmaceutically acceptable carrier. These compositionscan be prepared in a manner well known in the pharmaceutical arts, andcan be administered by a variety of routes, depending upon whether localor systemic treatment is desired and upon the area to be treated.Administration may be topical (including ophthalmic and to mucousmembranes including intranasal, vaginal and rectal delivery), pulmonary(e.g., by inhalation or insufflation of powders or aerosols, includingby nebulizer; intratracheal, intranasal, epidermal and transdermal),ocular, oral or parenteral. Methods for ocular delivery can includetopical administration (eye drops), subconjunctival, periocular orintravitreal injection or introduction by balloon catheter or ophthalmicinserts surgically placed in the conjunctival sac. Parenteraladministration includes intravenous, intraarterial, subcutaneous,intraperitoneal or intramuscular injection or infusion; or intracranial,e.g., intrathecal or intraventricular, administration. Parenteraladministration can be in the form of a single bolus dose, or may be, forexample, by a continuous perfusion pump. Pharmaceutical compositions andformulations for topical administration may include transdermal patches,ointments, lotions, creams, gels, drops, suppositories, sprays, liquidsand powders. Conventional pharmaceutical carriers, aqueous, powder oroily bases, thickeners and the like may be necessary or desirable.

This invention also includes pharmaceutical compositions which contain,as the active ingredient, one or more of the compounds of the inventionabove in combination with one or more pharmaceutically acceptablecarriers. In making the compositions of the invention, the activeingredient is typically mixed with an excipient, diluted by an excipientor enclosed within such a carrier in the form of, for example, acapsule, sachet, paper, or other container. When the excipient serves asa diluent, it can be a solid, semi-solid, or liquid material, which actsas a vehicle, carrier or medium for the active ingredient. Thus, thecompositions can be in the form of tablets, pills, powders, lozenges,sachets, cachets, elixirs, suspensions, emulsions, solutions, syrups,aerosols (as a solid or in a liquid medium), ointments containing, forexample, up to 10% by weight of the active compound, soft and hardgelatin capsules, suppositories, sterile injectable solutions, andsterile packaged powders.

In preparing a formulation, the active compound can be milled to providethe appropriate particle size prior to combining with the otheringredients. If the active compound is substantially insoluble, it canbe milled to a particle size of less than 200 mesh. If the activecompound is substantially water soluble, the particle size can beadjusted by milling to provide a substantially uniform distribution inthe formulation, e.g. about 40 mesh.

Some examples of suitable excipients include lactose, dextrose, sucrose,sorbitol, mannitol, starches, gum acacia, calcium phosphate, alginates,tragacanth, gelatin, calcium silicate, microcrystalline cellulose,polyvinylpyrrolidone, cellulose, water, syrup, and methyl cellulose. Theformulations can additionally include: lubricating agents such as talc,magnesium stearate, and mineral oil; wetting agents; emulsifying andsuspending agents; preserving agents such as methyl- andpropylhydroxy-benzoates; sweetening agents; and flavoring agents. Thecompositions of the invention can be formulated so as to provide quick,sustained or delayed release of the active ingredient afteradministration to the patient by employing procedures known in the art.

The compositions can be formulated in a unit dosage form, each dosagecontaining from about 5 to about 500 mg, more usually about 10 to about100 mg, of the active ingredient. The term “unit dosage forms” refers tophysically discrete units suitable as unitary dosages for human subjectsand other mammals, each unit containing a predetermined quantity ofactive material calculated to produce the desired therapeutic effect, inassociation with a suitable pharmaceutical excipient.

The active compound can be effective over a wide dosage range and isgenerally administered in a pharmaceutically effective amount. It willbe understood, however, that the amount of the compound actuallyadministered will usually be determined by a physician, according to therelevant circumstances, including the condition to be treated, thechosen route of administration, the actual compound administered, theage, weight, and response of the individual patient, the severity of thepatient's symptoms, and the like.

For preparing solid compositions such as tablets, the principal activeingredient is mixed with a pharmaceutical excipient to form a solidpreformulation composition containing a homogeneous mixture of acompound of the present invention. When referring to thesepreformulation compositions as homogeneous, the active ingredient istypically dispersed evenly throughout the composition so that thecomposition can be readily subdivided into equally effective unit dosageforms such as tablets, pills and capsules. This solid preformulation isthen subdivided into unit dosage forms of the type described abovecontaining from, for example, 0.1 to about 500 mg of the activeingredient of the present invention.

The tablets or pills of the present invention can be coated or otherwisecompounded to provide a dosage form affording the advantage of prolongedaction. For example, the tablet or pill can comprise an inner dosage andan outer dosage component, the latter being in the form of an envelopeover the former. The two components can be separated by an enteric layerwhich serves to resist disintegration in the stomach and permit theinner component to pass intact into the duodenum or to be delayed inrelease. A variety of materials can be used for such enteric layers orcoatings, such materials including a number of polymeric acids andmixtures of polymeric acids with such materials as shellac, cetylalcohol, and cellulose acetate.

The liquid forms in which the compounds and compositions of the presentinvention can be incorporated for administration orally or by injectioninclude aqueous solutions, suitably flavored syrups, aqueous or oilsuspensions, and flavored emulsions with edible oils such as cottonseedoil, sesame oil, coconut oil, or peanut oil, as well as elixirs andsimilar pharmaceutical vehicles.

Compositions for inhalation or insufflation include solutions andsuspensions in pharmaceutically acceptable, aqueous or organic solvents,or mixtures thereof, and powders. The liquid or solid compositions maycontain suitable pharmaceutically acceptable excipients as describedsupra. In some embodiments, the compositions are administered by theoral or nasal respiratory route for local or systemic effect.Compositions in can be nebulized by use of inert gases. Nebulizedsolutions may be breathed directly from the nebulizing device or thenebulizing device can be attached to a face masks tent, or intermittentpositive pressure breathing machine. Solution, suspension, or powdercompositions can be administered orally or nasally from devices whichdeliver the formulation in an appropriate manner.

The amount of compound or composition administered to a patient willvary depending upon what is being administered, the purpose of theadministration, such as prophylaxis or therapy, the state of thepatient, the manner of administration, and the like. In therapeuticapplications, compositions can be administered to a patient alreadysuffering from a disease in an amount sufficient to cure or at leastpartially arrest the symptoms of the disease and its complications.Effective doses will depend on the disease condition being treated aswell as by the judgment of the attending clinician depending uponfactors such as the severity of the disease, the age, weight and generalcondition of the patient, and the like.

The compositions administered to a patient can be in the form ofpharmaceutical compositions described above. These compositions can besterilized by conventional sterilization techniques, or may be sterilefiltered. Aqueous solutions can be packaged for use as is, orlyophilized, the lyophilized preparation being combined with a sterileaqueous carrier prior to administration. The pH of the compoundpreparations typically will be between 3 and 11, more preferably from 5to 9 and most preferably from 7 to 8. It will be understood that use ofcertain of the foregoing excipients, carriers, or stabilizers willresult in the formation of pharmaceutical salts.

The therapeutic dosage of the compounds of the present invention canvary according to, for example, the particular use for which thetreatment is made, the manner of administration of the compound, thehealth and condition of the patient, and the judgment of the prescribingphysician. The proportion or concentration of a compound of theinvention in a pharmaceutical composition can vary depending upon anumber of factors including dosage, chemical characteristics (e.g.,hydrophobicity), and the route of administration. For example, thecompounds of the invention can be provided in an aqueous physiologicalbuffer solution containing about 0.1 to about 10% w/v of the compoundfor parenteral adminstration. Some typical dose ranges are from about 1μg/kg to about 1 g/kg of body weight per day. In some embodiments, thedose range is from about 0.01 mg/kg to about 100 mg/kg of body weightper day. The dosage is likely to depend on such variables as the typeand extent of progression of the disease or disorder, the overall healthstatus of the particular patient, the relative biological efficacy ofthe compound selected, formulation of the excipient, and its route ofadministration. Effective doses can be extrapolated from dose-responsecurves derived from in vitro or animal model test systems.

The compounds of the invention can also be formulated in combinationwith one or more additional active ingredients which can include anypharmaceutical agent such as anti-viral agents, vaccines, antibodies,immune enhancers, immune suppressants, anti-inflammatory agents and thelike.

It is further appreciated that certain features of the invention, whichare, for clarity, described in the context of separate embodiments, canalso be provided in combination in a single embodiment. Conversely,various features of the invention which are, for brevity, described inthe context of a single embodiment, can also be provided separately orin any suitable subcombination.

The invention will be described in greater detail by way of specificexamples. The following examples are offered for illustrative purposes,and are not intended to limit the invention in any manner. Those ofskill in the art will readily recognize a variety of noncriticalparameters which can be changed or modified to yield essentially thesame results. The compounds of the Examples were found to be inhibitorsof c-Met according to one or more of the assays provided herein.

EXAMPLES

Experimental procedures for compounds of the invention are providedbelow. Generally, the product was purified on a preparative scale byhigh performance liquid chromatography (HPLC) or flash chromatography(silica gel) as indicated in the Examples. Typical preparativereverse-phase high performance liquid chromatography (RP-HPLC) columnconditions were as follows:

pH=2 purifications: Waters Sunfire™ C₁₈ 5 Tm, 19×100 mm column, elutingwith mobile phase A: 0.1% TFA (trifluoroacetic acid) in water and mobilephase B: 0.1% TFA in acetonitrile; the flow rate is 30 ml/m; theseparating gradient is optimized for each compound using the CompoundSpecific Method Optimization protocol as described in the literature[“Preparative LCMS Purification: Improved Compound Specific MethodOptimization”, K. Blom, B. Glass, R. Sparks, A. Combs, J. Comb. Chem.,6, 874-883 (2004)].

pH=10 purifications: Waters XBridge C₁₈ 5 Tm, 19×100 mm column, elutingwith mobile phase A: 0.15% NH₄OH in water and mobile phase B: 0.15%NH₄OH in acetonitrile; the flow rate was 30 ml/m; the separatinggradient is optimized for each compound using the Compound SpecificMethod Optimization protocol as described in the literature[“Preparative LCMS Purification: Improved Compound Specific MethodOptimization”, K. Blom, B. Glass, R. Sparks, A. Combs, J. Comb. Chem.,6, 874-883 (2004)].

The separated isomers were typically subjected to analytical liquidchromatography mass spectrometry (LCMS) for purity under the followingconditions: Instrument; Agilent 1100 series, LC/MSD, Column: WatersSunfire™ C₁₈ 5 Tm, 2.1×5.0 mm, Buffers: mobile phase A: 0.025% TFA inwater and mobile phase B: 0.025% TFA in acetonitrile; gradient 2% to 80%of B in 3 min with flow rate 1.5 mL/min.

Example 12-Fluoro-N-[(2R)-2-hydroxypropyl]-4-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]benzamide

Step 1: 4-Bromo-3-fluoro-N-methoxy-N-methylbenzamide

Oxalyl chloride (38.1 mL, 450 mmol) was slowly added to a mixture of4-bromo-3-fluorobenzoic acid (49.3 g, 225 mmol) (Alfa Aesar,Cat.#B25475) in dichloromethane (300 mL). Subsequently,N,N-dimethylformamide (1.0 mL) was added and the reaction mixture wasstirred at ambient temperature for 2 h. The reaction mixture wasconcentrated under reduced pressure and co-evaporated with toluene 3times. The residue was then dissolved in dichloromethane (100 mL). Thesolution was added drop-wise to a mixture of N,O-dimethylhydroxylaminehydrochloride (30.7 g, 315 mmol) and potassium carbonate (120 g, 900mmol) in dichloromethane (300 mL) and water (300 mL). The reactionmixture was stirred at ambient temperature for 2 hours. The organiclayer was separated. The aqueous layer was extracted withdichloromethane (2×50 mL). The combined organic extracts were washedwith brine, dried over magnesium sulfate, filtered and concentratedunder reduced pressure to give the product. (58.5 g) LCMS (M+H)⁺:m/z=261.9/263.9.

Step 2: 1-(4-Bromo-3-fluorophenyl)ethanone

To a solution of 4-bromo-3-fluoro-N-methoxy-N-methylbenzamide (Step 1,58.5 g, 223 mmol) in tetrahydrofuran (500 mL) was added 3M ofmethylmagnesium chloride in THF (125 mL, 380 mmol) at 0° C. The reactionmixture was stirred for 1 hour at 0° C., and was quenched with coldaqueous ammonium chloride solution (150 mL). The organic layer wasseparated and concentrated under reduced pressure. The residue wasre-dissolved in ethyl acetate (100 mL). The aqueous layer was dilutedwith water (100 mL) and was extracted with ethyl acetate (3×50 mL). Theorganic extracts were combined, washed with brine, and dried overmagnesium sulfate. Filtration and concentration under reduced pressuregave the product (48.4 g) which was used in the next reaction stepwithout further purification.

Step 3: (4-Bromo-3-fluorophenyl)(oxo)acetaldehyde and1-(4-bromo-3-fluorophenyl)-2,2-dihydroxyethanone

To a solution of 1-(4-bromo-3-fluorophenyl)ethanone (Step 2, 9.0 g, 41mmol) in dimethyl sulfoxide (40 mL) was added slowly a 48% aqueoussolution of hydrogen bromide.(14 mL) The reaction mixture was stirred at60° C. overnight and then cooled to ambient temperature, and poured intoice water. The precipitate was filtered and washed with water and thesolid was dried under vacuum overnight to obtain 8.1 g of desiredproduct. The aqueous layer was extracted with ethyl acetate 3 times. Thecombined extracts were washed with water, brine, dried, filtered, andconcentrated to give an additional 2.2 g of the desired product (10.3 gtotal).

Step 4: 1-(4-Bromo-3-fluorophenyl)-2,2-diethoxyethanone

To a mixture of 1-(4-bromo-3-fluorophenyl)-2,2-dihydroxyethanone and4-bromo-3-fluorophenyl)(oxo)acetaldehyde (crude product from Step 3, 7.0g, 28 mmol) in toluene (50 mL) was added ethyl orthoformate (12 mL, 70mmol) and p-toluenesulfonic acid (200 mg, 1 mmol). The reaction mixturewas refluxed for 4 h. The reaction mixture was cooled to RT, dilutedwith ethyl acetate, washed with aqueous sodium bicarbonate, water,brine, and dried over magnesium sulfate. Concentration under reducedpressure gave the desired product which was used in the next stepwithout further purification.

Step 5: 6-(4-Bromo-3-fluorophenyl)-1,2,4-triazin-3-amine

A mixture of 1-(4-bromo-3-fluorophenyl)-2,2-diethoxyethanone (Step 4,15.2 g, 50 mmol), aminoguanidine bicarbonate (10.2 g, 75 mmol) andpotassium hydroxide (6.6 g, 100 mmol) in ethanol (200 mL) and water (4mL) was refluxed overnight. The solvent was evaporated under reducedpressure and the residue was washed with acetonitrile and filtered. Thefiltrate was concentrated under reduced pressure. The residue wasdissolved in dichloromethane (100 mL), washed with water, brine, andconcentrated under reduced pressure. The residue was dissolved inethanol (50 mL). To the solution was added 0.2N hydrochloric acid (50mL). The resultant mixture was heated to 110° C. for 8 h, and cooledwith an ice-water bath. The precipitate that formed was collected byfiltration and washed with isopropanol to give the desired product. (5.5g, 41%) LCMS: (M+H)=286.8/288.8. ¹H-NMR (400 MHz, CDCl₃): 8.60 (s, 1H),7.79 (dd, J=8.6, 2.0 Hz, 1H), 7.68 (dd, J=8.3, 7.0 Hz, 1H), 7.61 (dd,J=8.3, 2.0 Hz, 1H), 5.43 (s, 2H).

Step 6: 3-Quinolin-6-ylpropanal

Tris(dibenzylideneacetone)dipalladium (480 mg, 0.52 mmol) (Aldrich, Cat.#328774) and tri-tent-butyl-phosphonium tetrafluoroborate (300mg, 1.0mmol) in a flask was evacuated and refilled with nitrogen (2 times).1,4-Dioxane (31 mL) was added followed by consecutive addition of6-bromoquinoline (7.2 g, 35 mmol) (TCI, Cat. #B2015), 2-propen-1-ol (4.7mL, 69 mmol) and N-cyclohexyl-N-methyl-cyclohexanamine (8.9 mL, 42mmol). The reaction vessel was evacuated and refilled with nitrogen (2times). The reaction mixture was stirred at 30° C. for 24 h. Diethylether (30 mL) was added to the reaction mixture and then filtered andwashed with diethyl ether. The organic extract was concentrated underreduced pressure. The residue was purified by flash chromatographyeluting with ethyl acetate in hexanes (0-50%) to afford the desiredproduct. (˜55%) LCMS (M+H)⁺: m/z=186.0; (M+H₂O+H)⁺: m/z=204.0.

Step 7:1-(2-Chloro-1-hydroxy-3-quinolin-6-ylpropyl)pyrrolidine-2,5-dione

To a solution of 3-quinolin-6-ylpropanal (Step 6, 2.3 g, 0.012 mol) inchloroform (5 mL) cooled at 0° C. was added L-proline (0.4 g, 0.004mol). To the mixture was then added N-chlorosuccinimide (1.74 g, 0.0130mol) at 0° C. The reaction was warmed to r.t. and stirred overnight. Thereaction was thick slurry. Solid was filtered and was washed withchloroform to give the pure product (2 g, 50.5%). ¹H-NMR (300 MHz,CDCl₃): 8.90 (dd, J=4.0, 2.0 Hz, 1H), 8.13 (d, J=8.0 Hz, 1H), 8.05 (d,J=8.4 Hz, 1H), 7.73 (s, 1H), 7.65 (dd, J=8.0, 2.0 Hz, 1H), 7.40 (dd,J=8.4, 4.0 Hz, 1H), 5.46 (d, J=9.4 Hz, 1H), 4.95 (ddd, J=9.4, 8.0, 3.1Hz, 1H), 3.73 (dd, J=14.3, 3.1 Hz, 1H), 3.19 (dd, J=14.3, 8.0 Hz, 1H),2.75 (s, 4H).

Step 8:6-[2-(4-Bromo-3-fluorophenyl)imidazo[1,2-b][1,2,4]triazin-7-yl]methylquinoline

A mixture of 6-(4-bromo-3-fluorophenyl)-1,2,4-triazin-3-amine (Step 5,200 mg, 0.743 mmol) and1-(2-chloro-1-hydroxy-3-quinolin-6-ylpropyl)pyrrolidine-2,5-dione (Step7, 284 mg, 0.892 mmol) in isopropyl alcohol (7.4 mL) and water (0.11 mL)in a sealed tube was heated at 105° C. for 5 d. After the reactionmixture was cooled to ambient temperature, the precipitate was collectedby filtration, washed with isopropanyl alcohol, and dried in vacuum togive the desired product (180 mg, 55%) LCMS (M+H)⁺: m/z=433.9/436.0.

Step 9:2-Fluoro-4-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]benzonitrile

Zinc cyanide (131 mg, 1.11 mmol),tris(dibenzylideneacetone)dipalladium(0) (35 mg, 0.038 mmol) (Aldrich,Cat. #328774),(9,9-dimethyl-9H-xanthene-4,5-diyl)bis-(diphenylphosphine) (78.5 mg,0.136 mmol) (Aldrich, Cat. #526460), andN,N,N′,N′-tetramethylethylenediamine (0.22 mL, 1.4 mmol) were addedsuccessively to a mixture of6-[2-(4-bromo-3-fluorophenyl)imidazo[1,2-b][1,2,4]-triazin-7-yl]methylquinoline(Step 8, 480 mg, 1.10 mmol) in N,N-dimethylformamide (8.7 mL) in amicrowave tube. The tube was sealed and degassed three times and heatedto 160° C. under microwave irradiation for 500 s. Most of the solventwas removed under reduced pressure and the residue was dissolved inethyl acetate, washed with aqueous sodium bicarbonate, water and brine,and dried over magnesium sulfate. Filtration and concentration affordeda residue which was purified on a silica gel column with methanol indichloromethane (0-6%) to give the desired product. (90%) LCMS (M+H)⁺:m/z=381.0.

Step 10:2-Fluoro-4-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]benzoicacid

2-Fluoro-4-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]benzonitrile(Step, 9, 750 mg, 2 mmol) in a concentrated solution of hydrochloricacid (5.0 mL, 53 mmol) and water (1.0 mL) was stirred at 105° C.overnight. The solvent was removed under reduced pressure and theresultant residue was washed with water and filtered to provide thecrude product as the HCl salt which was directly used in next reactionstep without further purification. LCMS (M+H)⁺: m/z=400.0.

Step 11:2-Fluoro-N-[(2R)-2-hydroxypropyl]-4-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]benzamide

A mixture of2-fluoro-4-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]benzoicacid HCl salt (180.0 mg, 0.381 mmol, Step 10) andbenzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate(220 mg, 0.50 mmol) (Aldrich, Cat. #226084) in N,N-dimethylformamide(9.0 mL) was stirred at r.t. for 3 min. (2R)-1-Aminopropan-2-ol (57 mg,0.76 mmol) was then slowly added followed by triethylamine (318.7 μL,2.287 mmol). The mixture was stirred at r.t. for 3 h., and then waterwas added. The precipitate was collected by filtration and washed withaqueous acetonitrile. The precipitate was dissolved in 1 N HCl aqueoussolution, and then dried by lyophilization to give the desired productas the HCl salt. LCMS (M+H)⁺: m/z=457.3. ¹H-NMR (500 MHz, DMSO-d₆): 9.30(s, 1H), 9.20 (dd, J=5.0, 1.5 Hz, 1H), 9.02 (d, J=8.0 Hz, 1H), 8.37 (s,1H), 8.35 (d, J=8.0 Hz, 1H), 8.28 (s, 1H), 8.16 (dd, J=8.5, 1.5 Hz, 1H),8.08 (s, 1H), 8.04 (s, 1H), 8.02 (s, 1H), 8.00 (dd, J=8.5, 5.0, Hz, 1H),7.80 (t, J=8.0 Hz, 1 H), 4.75 (s, 2H), 3.79 (m, 1H), 3.21 (m, 2H), 1.09(d, J=7.0 Hz, 3H).

The S enantiomer can be made according to the above procedure using(2S)-1-aminopropan-2-ol or by racemizing the product and separatingenantiomers using standard chiral separation techniques (e.g., a chiralcolumn).

Example 22-Chloro-N-methyl-4-(7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl)benzamide

Step 1: 6-Bromo-1,2,4-triazin-3-amine

To a suspension of 1,2,4-triazin-3-amine (3.84 g, 40.0 mmol) (Aldrich,Cat. #100625) in acetonitrile (40 mL) was added water (60 mL) andstirred until a clear solution was formed. To this solution was addedN-bromosuccinimide (7.48 g, 42.0 mmol) at 0° C. and the resultingmixture was stirred for 10 min. The cooling bath was removed, and themixture was allowed to warm to room temperature. The mixture was thendiluted with ethyl acetate (150 mL) and cooled to 0° C. (ice-waterbath). Na₂CO₃ (3.0 g) was added and stirred for 10 min. The two layerswere separated and the aqueous phase was extracted with ethyl acetate(150 mL). The combined organic layers were washed with sat'd NaHCO₃,brine, dried over MgSO₄, and filtered. The filtrate was concentratedunder reduced pressure to afford the desired product (4 g, 57.15%). LCMS(M+H)⁺: m/z=175.2/177.2.

Step 2: Methyl 4-(3-amino-1,2,4-triazin-6-yl-2-chlorobenzoate

To a mixture of 6-bromo-1,2,4-triazin-3-amine (Step 1, 1.0 g, 5.7 mmol)and [3-chloro-4-(methoxycarbonyl)phenyl]boronic acid (1.5 g, 6.8 mmol)(VMR, Cat. #100013-404) in 1,4-dioxane (22 mL) was added a solution ofpotassium phosphate (2.4 g, 11 mmol) in water (5.1 mL). The mixture wasdegassed by purging nitrogen for 10 min. To the mixture was addedtetrakis(triphenylphosphine)palladium(0) (0.20 g, 0.17 mmol) and againwas degassed with nitrogen. The mixture was stirred and heated at 82° C.(an oil bath) for 1 h. The mixture was cooled to r.t., diluted withwater, stirred for 30 min, and a grey solid formed. The solid wasisolated by filtration, rinsed several times with water, and dried inair. The solid was then triturated sequentially with hexanes,dichloromethane-hexanes (1:1), and hexanes to afford the desired product(840 mg, 55.54%). LCMS (M+H)⁺: m/z=264.9/267.0.

Step 3: Methyl2-chloro-4-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]benzoate

The mixture of methyl 4-(3-amino-1,2,4-triazin-6-yl)-2-chlorobenzoate(Step 2, 0.840 g, 3.17 mmol) and1-(2-chloro-1-hydroxy-3-quinolin-6-ylpropyl)pyrrolidine-2,5-dione (1.11g, 3.49 mmol, Example 1, Step 7) in 1-butanol (11.6 mL) was stirred at110° C. for 22 h. The solvent was removed under reduced pressure. Theresidue was triturated with ethyl acetate. The precipitate was collectedby filtration and washed with ethyl acetate and hexane to yield thedesired product (0.908 g). The mother liquor was concentrated to halfvolume. The precipitate was collected by filtration and washed withethyl acetate and hexane to afford additional desired product (0.342 g).The total product obtained was 1.10 g (80.6%). LCMS (M+H)⁺:m/z=430.0/431.9.

Step 4:2-Chloro-4-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]benzoicacid

To a solution of methyl2-chloro-4-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]benzoate(Step 3, 1.10 g, 2.56 mmol) in tetrahydrofuran (7.0 mL) and methanol(5.0 mL) was added a solution of lithium hydroxide (0.245 g, 10.2 mmol)in water (3.0 mL). The mixture was stirred at room temperature for 2 h.and concentrated under reduced pressure to a volume of about 3 mL. Theresidue was diluted with water (3 mL), and adjusted with 1N HCl to pH ofabout 4-5. The precipitate was filtered out, washed several times withwater and dried in air overnight. The precipitate was then trituratedsequentially with ether and dichloromethane (DCM)-Hexane (1:1). Thedesired product (638 mg, 60%) was obtained. LCMS (M+H)⁺:m/z=415.9/417.9.

Step 5:2-Chloro-N-methyl-4-(7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl)benzamide

2-Chloro-4-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]benzoicacid (Step 4, 5.0 mg, 0.012 mmol) and(benzotriazol-1-yloxy)tripyrrolidinophosphonium hexafluorophosphate(10.0 mg, 0.020 mmol) (Aldrich, Cat. #226084) in N,N-dimethylformamide(0.5 mL) was stirred at r.t. for 3 min. 2.0 M of Methylamine intetrahydrofuran (0.012 mL, 0.023 mmol) was then slowly added at 0° C.followed by triethylamine (6.4 μL, 0.046 mmol). The mixture was stirredat r.t. for 2 h., and purified by RP-HPLC (pH=2) to afford the desiredproduct as the trifluoroacetate (TFA) salt. LCMS (M+H)⁺: m/z=429.3.

Example 32-Chloro-N-[(1S)-1-(5-methyl-1,2,4-oxadiazol-3-yl)ethyl]-4-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]benzamide

Step 1: tert-Butyl [(1S)-2-amino-1-methyl-2-oxoethyl]carbamate

To a stirred solution of (2S)-2-[(tert-butoxycarbonyl)amino]propanoicacid (1 g, 0.005 mol) in THF at 0° C. was added 4-methylmorpholine(0.588 g, 0.00581 mol) followed by dropwise addition of isobutylchloroformate (0.794 g, 0.00581 mol) over 2 min. The reaction wasstirred at 0° C. for 30 min. after which a solution of 30 wt. % ammoniumhydroxide (12.0 mL, 0.0925 mol) was quickly poured into the reaction.The reaction was warmed to room temperature and stirred for 5 h. Thereaction mixture was concentrated. Water was added and the mixtureextracted with ethyl acetate. The combined organic layers were washedwith brine, dried over MgSO₄, filtered and concentrated to afford thecrude product which was directly used in the next step reaction withoutfurther purification (800 mg, 80%). ¹H-NMR (300 MHz, DMSO-d₆): 12.40 (s,1H), 7.10 (d, J=7.0 Hz, 1H), 3.88 (m, 1H), 1.35 (s, 9H), 1.20 (d, J=7.3Hz, 3H).

Step 2: tert-Butyl [(1S)-1-cyanoethyl]carbamate

To a stirred solution of tert-butyl[(1S)-2-amino-1-methyl-2-oxoethyl]carbamate (Step 1, 0.7 g, 0.004 mol)in N,N-dimethylformamide (5 mL) was added 343 mg of cyanuric chloride(0.00186 mol) at once. The reaction mixture was stirred for 4 h. Waterwas added and the mixture was extracted with ethyl acetate. The combinedorganic layers were washed with brine, dried over MgSO₄, filtered, andconcentrated under reduced pressure. The residue was purified by flashchromatography on a silica gel column with EtOAc in hexane (30-50%) toyield the desired product (400 mg, 63%). ¹H-NMR (300 MHz, DMSO-d₆): 7.74(d, J=7.0 Hz, 1H), 4.48 (m, 1H), 1.40 (s, 9H), 1.35 (d, J=7.0 Hz, 3H).

Step 3: tert-Butyl[(1S,2Z)-2-amino-2-(hydroxyimino)-1-methylethyl]carbamate

To a mixture of tert-butyl [(1S)-1-cyanoethyl]carbamate (Step 2, 250 mg,1.5 mmol) in ethanol (3 mL) were added triethylamine (0.41 mL, 2.9 mmol)and hydroxylamine (58 mg, 1.8 mmol). The mixture was stirred at 50° C.overnight. The reaction mixture was concentrated to afford the desiredcrude product (300 mg) which was directly used in the next step reactionwithout further purification. ¹H-NMR (300 MHz, DMSO-d₆): 8.94 (s, 1H),6.80 (d, J=8.5 Hz, 1H), 5.24 (s, 2H), 4.01 (m, 1H), 1.36 (s, 9H), 1.15(d, J=7.0 Hz, 3H).

Step 4: tert-Butyl{(1S,2Z)-2-[(acetyloxy)imino]-2-amino-1-methylethyl}carbamate

To a mixture of tert-butyl[(1S,2Z)-2-amino-2-(hydroxyimino)-1-methylethyl]carbamate (Step 3, 100mg, 0.5 mmol) in methylene chloride (2 mL) cooled at 0° C. was addedtriethylamine (0.10 mL, 0.74 mmol). To the mixture was then added acetylchloride (42 mg, 0.54 mmol) dropwise and the reaction was warmed to roomtemperature. After stirring at room temperature for 1 h, the reactionwas concentrated. The residue was dissolved in dichloromethane (DCM),washed with water and brine, dried over MgSO₄, filtered and concentratedto afford the desired crude product (100 mg, 82.8%) which was directlyused in the next step reaction without further purification. ¹H-NMR (300MHz, DMSO-d₆): 6.90 (d, J=9.0 Hz, 1H), 6.22 (s, 2H), 4.05 (m, 1H), 2.01(s, 3H), 1.36 (s, 9H), 1.20 (d, J=7.0 Hz, 3H).

Step 5: (1S)-1-(5-Methyl-1,2,4-oxadiazol-3-ethanamine

To a solution of tert-butyl{(1S,2Z)-2-[(acetyloxy)imino]-2-amino-1-methylethyl}carbamate (Step 4,80 mg, 0.3 mmol) in ethanol (3 mL) was added a solution of sodiumacetate trihydrate (49 mg, 0.36 mmol) in water (1 mL). The mixture washeated at 85° C. for 3 h. Ethanol was evaporated; water was added andextracted with EtOAc. The combined organic layers were washed withbrine, dried over MgSO₄, filtered and concentrated. The residue wasdissolved in methylene chloride (1 mL). To the solution was addedtrifluoroacetic acid (1 mL). After stirring 30 min., the reactionmixture was concentrated to afford the desired product as TFA salt whichwas directly used in the next step reaction without further purification

Step 6:2-Chloro-N-[(1S)-1-(5-methyl-1,2,4-oxadiazol-3-yl)ethyl]-4-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]benzamide

To a solution of2-chloro-4-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]benzoicacid (50 mg, 0.1 mmol, Example 2, Step 4) in N,N-dimethylformamide (2mL, 20 mmol) was addedN,N,N′,N′-tetramethyl-O-(7-azabenzotriazol-1-yl)uroniumhexafluorophosphate (68 mg, 0.18 mmol) (Aldrich, Cat. #226084) andN,N-diisopropylethylamine (42 μL, 0.24 mmol). After stirring thesolution for 15 min, (1S)-1-(5-methyl-1,2,4-oxadiazol-3-yl)ethanamineTFA salt (18 mg, 0.14 mmol, Step 5) was added and stirred overnight. Themixture was purified by RP-HPLC (pH=10) to give the desired productwhich was further purified by RP-HPLC (pH=2) to afford the desired pureproduct as the TFA salt. LCMS (M+H)⁺: m/z=525.0/427.0. ¹H-NMR (500 MHz,DMSO-d₆): 9.22 (s, 1H), 8.98 (dd, J=5.0, 1.5 Hz, 1H), 9.15 (d, J=8.0 Hz,1H), 8.56 (d, J=8.5 Hz, 1H), 8.16 (d, J=2.0 Hz, 1H), 8.14 (dd, J=8.0,1.5 Hz, 1H), 8.06 (s, 1H), 8.04 (d, J=9.0 Hz, 1H), 8.02 (s, 1H), 7.90(dd, J=9.0, 2.0 Hz, 1H), 7.68 (dd, J=8.5, 5.0 Hz, 1H), 7.60 (d, J=8.0Hz, 1 H), 5.24 (m, 1H), 4.66 (s, 2H), 2.60 (s, 3H), 1.51 (d, J=7.0 Hz,3H).

The R enantiomer can be made according to the above procedure using(1R)-1-(5-methyl-1,2,4-oxadiazol-3-yl)ethanamine or by racemizing theproduct and separating enantiomers using standard chiral separationtechniques (e.g., a chiral column).

Example 4N-Methyl-5-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]pyridine-2-carboxamide

Step 1: 5-(3-Amino-1,2,4-triazin-6-yl)-N-methylpyridine-2-carboxamide

A mixture ofN-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-2-carboxamide(200 mg, 0.80 mmol) (VWR, Cat. #200068-640),6-bromo-1,2,4-triazin-3-amine (130 mg, 0.76 mmol, Example 2, Step 1),tetrakis(triphenylphosphine)palladium(0) (40 mg, 0.04 mmol) andpotassium carbonate (0.32 g, 2.3 mmol) in toluene (1.3 mL), ethanol(0.66 mL) and water (0.66 mL) was heated at 120° C. for 1.5 h. Themixture was filtered and washed with methanol. The filtrate was purifiedby RP-HPLC (pH=10) to afford the desired product (80 mg, 45.54%). LCMS(M+H)⁺: m/z=231.4; LCMS (M+H+H₂O)⁺: m/z=249.3.

Step 2:N-Methyl-5-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]pyridine-2-carboxamide

A mixture of5-(3-amino-1,2,4-triazin-6-yl)-N-methylpyridine-2-carboxamide (Step 1,6.5 g, 0.022 mol) and1-(2-chloro-1-hydroxy-3-quinolin-6-ylpropyl)pyrrolidine-2,5-dione (8.71g, 0.0273 mol, Example 1, Step 7) in 1,2-ethanediol (100 mL) was stirredat 120° C. overnight. The reaction mixture was concentrated. The mixturewas neutralized to pH=10 with methylamine in THF solution (2.0M), andthen purified by flash chromatography on a silica gel column with 5%MeOH in dichloromethane to afford the desired product which wascontaminated with some starting material. The product was dissolved in10% MeOH in dichloromethane, and concentrated to a volume of about 2 mL.The resulted solid was filtered, washed with MeOH (2 mL) to afford thepure product (4.50 g, 50%). The product was treated with 2N HCl(aqueous) and acetonitrile, and dried by lyophilization to give thedesired product as the HCl salt. LCMS (M+H)⁺: m/z=396.4. ¹H-NMR (400MHz, DMSO-d₆): 9.40 (s, 1H), 9.27 (s, 1H), 9.20 (d, J=5.5 Hz, 1H), 9.10(d, J=8.0 Hz, 1H), 8.64 (d, J=8.0 Hz, 1H), 8.30 (s, 1H), 8.26 (d, J=8.0Hz, 1H), 8.20 (d, J=8.0, Hz, 1H), 8.19 (s, 1H), 8.17 (d, J=8.0 Hz, 1H),7.03 (dd, J=8.0, 5.5 Hz, 1 H), 4.76 (s, 2H), 2.81 (s, 3H).

Example 5N,2-Dimethyl-4-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]benzamide

Step 1: 4-Bromo-N,2-dimethylbenzamide

N,N-Dimethylformamide (10 μL) was added to a mixture of4-bromo-2-methylbenzoic acid (1.0 g, 4.6 mmol) in oxalyl chloride (2.0mL, 23 mmol). The mixture was stirred at room temperature overnight. Themixture was concentrated to afford a crude carbonyl chloride which wasdissolved in methylene chloride (2 mL). The solution was added slowly toa mixture of methylamine in tetrahydrofuran (THF) (2.0 M, 0.465 mL, 9.3mmol) and triethylamine (1.3 mL, 9.3 mmol) in DCM (10 ml). After 30 min,the reaction mixture was quenched with sat. sodium carbonate (10 mL) andextracted with DCM (3×20 mL). The combined organic layers were washedwith brine, dried over Na₂SO₄, filtered, concentrated under reducedpressure to give a crude product (980 mg, 92%). LCMS (M+H)⁺:m/z=228.1/230.2.

Step 2:N,2-Dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide

To a solution of 4-bromo-N,2-dimethylbenzamide (Step 1, 0.50 g, 2.2mmol) and 4,4,5,5,4′,4′,5′,5′-octamethyl-[2,2′]bi[[1,3,2]dioxaborolanyl](0.67 g, 2.6 mmol) (Aldrich, Cat. #473294) in 1,4-dioxane (5.28 mL) wasadded [1,1′-bis(diphenylphosphino)-ferrocene]dichloropalladium(II)complex with dichloromethane (1:1) (0.09 g, 0.1 mmol) (Aldrich, Cat.#379670), potassium acetate (0.64 g, 0.0066 mol), and1,1′-bis(diphenylphosphino)ferrocene (0.06 g, 0.1 mmol) (Aldrich, Cat.#177261) under an atmosphere of nitrogen. The reaction mixture wasstirred at 80° C. overnight. After cooling to room temperature, themixture was filtered, and concentrated under reduced pressure. Theresidue was purified by flash chromatography on a silica gel column with10% methanol in dichloromethane to afford the desired product. LCMS(M+H)⁺: m/z=276.4.

Step 3: 4-(3-Amino-1,2,4-triazin-6-yl)-N,2-dimethylbenzamide

A mixture ofN,2-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide(Step 2, 0.3 g, 0.001 mol), 6-bromo-1,2,4-triazin-3-amine (0.21 g, 1.2mmol, Example 2, Step 1), tetrakis(triphenylphosphine)palladium(0) (0.06g, 0.05 mmol) and potassium carbonate (0.45 g, 3.3 mmol) in toluene (1.9mL), ethanol (0.94 mL) and water (0.94 mL). The resulting mixture washeated at 130° C. for 2.5 h. The mixture was diluted with MeOH,filtered, and washed with DCM/methanol (90%). The filtrate wasconcentrated. The residue was purified by flash chromatography on asilica gel column with 10% MeOH in DCM to afford the desired product(110 mg, 41%). LCMS (M+H)⁺: m/z=244.3.

Step 4: 2-Chloro-3-quinohn-6-ylpropanal

L-Proline (410 mg, 3.5 mmol) was added to a solution of3-quinolin-6-ylpropanal (3.27 g, 17.6 mmol, Example 1, Step 6) inchloroform (39 mL) at 0° C. followed by addition of N-chlorosuccinimide(2.48 g, 18.5 mmol) and the reaction mixture was slowly warmed toambient temperature and stirred for 1 h, monitoring by LCMS. The solventwas concentrated under reduced pressure and the residue was purified ona silica gel column with ethyl acetate in hexane (0-50%) to give thedesired product. (95%) LCMS: (M+H+H₂O)=237.9/239.9.

Step 5:N,2-Dimethyl-4-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]benzamide

A mixture of 4-(3-amino-1,2,4-triazin-6-yl)-N,2-dimethylbenzamide (Step3, 0.30 g, 1.2 mmol) and 2-chloro-3-quinolin-6-ylpropanal (Step 4, 0.32g, 1.5 mmol) in ethanol (2.5 mL) in a sealed tube was stirred at 120° C.overnight. After cooling, the reaction mixture was purified by RP-HPLC(pH=2) to afford the desired product (150 mg) as the TFA salt. LCMS(M+H)⁺: m/z=409.3. ¹H-NMR (400 MHz, CD₃OD): 9.64 (s, 1H), 9.21 (d,J=5.0, 1H), 9.18 (d, J=8.0 Hz, 1H), 8.44 (s, 1H), 8.39 (s, 1H), 8.32 (d,J=9.0 Hz, 1H), 8.27 (d, J=8.0 Hz, 1H), 8.12 (dd, J=9.0, 5.0, Hz, 1H),8.05 (s, 1H), 8.03 (s, 1H), 7.57 (d, J=8.0 Hz, 1 H), 4.86 (s, 2H), 2.92(s, 3H), 2.48 (s, 3H).

Example A In Vitro c-Met Kinase Enzyme Assays

The compounds of the invention were screened in vitro for their abilityto inhibit c-Met kinase activity. The IC₅₀ values for the inhibition ofc-Met kinase were determined as described in the literature with somemodifications (Wang, X. et al, Mol. Cancer Ther. 2003, 2(11):1085-1092;Calic, M. et al., Croatica Chemical ACTA. 2005, 78(3):367-374). Briefly,histidine-tagged c-Met catalytic domain fusion protein (Invitrogen,#PV3143) was used for the assay. IC₅₀ measurements were based on thedegree of phosphorylation of poly Glu-Tyr (Sigma-Aldrich, #P0275) thatwas coated (0.01 mg/per well) on 96-well microplates (R&D systems,#DY990). The reaction was carried out in a 50 μL solution containing 50mM HEPES (pH 7.5), 10 mM MnCl₂, 10 mM MgCl₂, 0.5 mM DTT, 100 μM Na₃VO₄,5 μM ATP (Cell Signaling Technology, #9804) and serial dilutions of thetest compound. The reaction lasted for 25 minutes at 30° C. After thereaction was completed, the contents of the plates were discarded.Plates were then washed with TBS-T (250 μL/well, 5×) and then blockedwith TBS-T containing 1% BSA for 2 hours. The contents of the plates wasdiscarded, and 100 μL (per well) of peroxidase-labeledanti-phospho-tyrosine antibody (Sigma, #A5964) diluted (1:60,000) in 1%BSA containing TBS-T were then added and incubated for 1 hour. Plateswere washed with TBS-T (250 μL/well, 5×) and followed by the colorreaction using 100 μL (1:1 mixture) of H₂O₂ and tetramethylbenzidine(R&D Systems, #DY999). The reaction was stopped in minutes with 100 μLof 2 N H₂SO₄. The optical density was measured immediately using amicroplate reader at 450 nm with wavelength correction at 540 nm. IC₅₀values were calculated with the GraphPad Prism software. The linearrange (i.e., the time period over which the rate remained equivalent tothe initial rate) was determined for the kinase and IC₅₀ determinationswere performed within this range.

Wang, X., et al. Potent and selective inhibitors of the Met [hepatocytegrowth factor/scatter factor (HGF/SF) receptor] tyrosine kinase blockHGF/SF-induced tumor cell growth and invasion. Mol. Cancer Ther. 2003,2(11):1085-1092.

Calic, M., et al. Flavonoids as inhibitors of Lck and Fyn kinases.Croatica Chemica ACTA. 2005, 78(3):367-374.

The IC₅₀ results for the compounds of the invention are shown below:

Compound IC₅₀ Formula I 0.1-1.0 nM Formula II 0.1-1.0 nM Formula III0.1-1.0 nM Formula IV 0.1-1.0 nM Formula V 0.1-1.0 nM

Example B Cell Proliferation/Survival Assays

Cell lines representing various human cancers (SNU-1 and SUN-5 gastric,A549 and NCI-H441 lung, U-87 glioblastoma, HT-29 colon, 786-O kidney,PC-3 pancreatic) can be obtained from American Type Culture Collectionand routinely maintained in culture media and conditions recommended byATCC. Optimal cell density used in proliferation/survival assay can bepredetermined for individual cell lines. Compounds are screened fortheir ability to inhibit cell proliferation/survival, and IC₅₀ valuesare determined. Below are the sample protocols for SNU-5 and SNU-1 cellproliferation/survival assays. SNU-5 and SNU-1 cells are seeded into 96well cell culture plates at 4000 cells/well and 2000 cells/wellrespectively in appropriate media containing 2% FBS and supplementedwith serial dilutions of individual compounds in a final volume of 100μL/well. After 72 hour incubation, 24 μL, of CellTiter 96® AQueous OneSolution reagent (Promega, #G3581) are added to each well (finalconcentration=333 μg/mL), and the plates are incubated for 2 more hoursin a 37° C. incubator. The optical density is measured in the linearrange using a microplate reader at 490 nm with wavelength correction at650 nm. IC₅₀ values are calculated with the GraphPad Prism software. Forproliferation assays using A549, NCI-H441, U-87, HT-29, 786-0 and PC-3cells, the cells are first starved for 48 hours in low serum condition(0.1-0.5% FBS in appropriate culture media), then treated with differentconcentrations of compounds for 2 hours. After the cells are treatedwith HGF (50 ng/mL) (R&D, #294-HGN) for 24 hours, CellTiter 96® AQueousOne Solution reagent is added and plates are incubated for 2 hours. Theresults are recorded with a plate reader.

Example C Cell-Based c-Met Phosphorylation Assays

The inhibitory effect of compounds on c-Met phosphorylation in relevantcell lines (SNU-5 gastric, A549 and NCI-H441 lung, U-87 glioblastoma,HT-29 colon, 786-O kidney and PC-3 pancreatic cancer cell lines andHUVEC cell line) can be assessed using immunoblotting analysis andELISA-based c-Met phosphorylation assays. Cells are grown in appropriateculture media and treated with various concentrations of individualcompounds. For SNU-5, HT-29, 786-0 cells, cells are grown inappropriated media supplemented with 0.2% or 2% FBS and treated withcompounds for 3-4 hours. Whole cell protein extracts are prepared usingreagents and a protocol (#FNN0011) obtained from Biosource Internationalwith slight modifications. Briefly, protein extracts are made byincubation in lysis buffer with protease and phosphatase inhibitors [50mM HEPES (pH 7.5), 100 mM NaCl, 1.5 mM MgCl₂, 10% Glycerol, 1% TritonX-100, 1 mM sodium orthovanadate, 1 mM sodium fluoride, aprotinin (2μg/mL), leupeptin (2 μg/mL), pepstatin A (2 μg/mL), andphenylmethylsulfonyl fluoride (1 mM)] at 4° C. Protein extracts arecleared of cellular debris by centrifugation at 14,000×g for 20 minutes.For A549, H441, U-87 and PC-3 cells, cells are serum (0.2% FBS) starvedfor at least 24 hours, then pretreated with various concentrations ofcompounds for 1 hour. Whole cell extracts are prepared after the cellswere treated with HGF (50 ng/mL) for 10 minutes.

Immunoblotting Analysis

Relevant antibodies are obtained from commercial sources: rabbitpolyclonal antibodies included anti-human c-Met (Santa CruzBiotechnology, #sc-161) and anti-phosphorylated-c-Met (BiosourceInternational, pY1230/4/5 and pY1003). For immunoblotting, 10-20 μg ofprotein extracts from individual treatment conditions are resolved byelectrophoresis on 10% SDS-PAGE gel, and electrotransferred to anitrocellulose (or PVDF) membrane. The membrane is blocked in PBScontaining 3% milk and 0.1% Tween-20 for 1 hour, and then incubated withprimary anti-c-Met antibodies in blocking solution for 1 hour. After 3washes, the membrane is incubated with appropriatehorseradish-conjugated secondary antibodies for 1 hour. After finalwash, the blot is incubated with chemiluminescence detection reagent for5 minutes and exposed to X-ray film. The images are scanned, quantifiedand corrected with total c-Met, and IC₅₀ values are calculated.Compounds having an IC₅₀ of 10 μM or less are considered active.

ELISA

Cell protein extracts are analyzed using a human phospho-c-Met ELISA kitaccording to the manufacturer's instructions (R&D Systems, #DYC2480).Optimal amounts of protein extracts are predetermined for individualcell lines. Briefly, for the assay, appropriate amounts of proteinextracts are captured with a capture anti-human c-Met antibody for 2hours in a 96 well microplate. After washes, a detection antibody(HRP-conjugated anti-phospho-tyrosine antibody) is added and incubatedfor 2 hours. After additional washes, 100 μL of substrate solution (1:1mixture of H₂O₂ and tetramethylbenzidine) are added into each well andthe reaction is stopped with 2 N H₂SO₄ within an appropriate amount oftime during color development. The optical density is measured in thelinear range using a microplate reader at 450 nm with wavelengthcorrection at 540 nm. IC₅₀ values are calculated with the GraphPad Prismsoftware.

Various modifications of the invention, in addition to those describedherein, will be apparent to those skilled in the art from the foregoingdescription. Such modifications are also intended to fall within thescope of the appended claims. Each reference, including all patent,patent applications, and publications, cited in the present applicationis incorporated herein by reference in its entirety.

1-14. (canceled)
 15. A method of inhibiting the HGF/c-MET signalingpathway in a cell comprising contacting said cell with a compound of2-fluoro-N-[(2R)-2-hydroxypropyl]-4-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]benzamide;or a pharmaceutically acceptable salt thereof.
 16. A method of treatinggastric cancer, cancer of the kidney, liver cancer, lung cancer, orglioblastoma in a patient comprising administering to said patient atherapeutically effective amount of2-fluoro-N-[(2R)-2-hydroxypropyl]-4-[7-(quinolin-6-ylmethyl)imidazo[1,2-b][1,2,4]triazin-2-yl]benzamide;or a pharmaceutically acceptable salt thereof.
 17. The method of claim15, wherein said cancer is gastric cancer.
 18. The method of claim 15,wherein said cancer is cancer of the kidney.
 19. The method of claim 15,wherein said cancer is liver cancer.
 20. The method of claim 15, whereinsaid cancer is lung cancer.
 21. The method of claim 15, wherein saidcancer is glioblastoma.
 22. The method of claim 16, wherein said canceris gastric cancer.
 23. The method of claim 16, wherein said cancer iscancer of the kidney.
 24. The method of claim 16, wherein said cancer isliver cancer.
 25. The method of claim 16, wherein said cancer is lungcancer.
 26. The method of claim 16, wherein said cancer is glioblastoma.